Canonical Allele Identifier: PA2827976016
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp1105Glu
CA16028782
NM_001354899.2:c.3315T>A
CA16028783
NM_001354899.2:c.3315T>G